Evidence map›Paper›PMID 38485764›Full record

ArticleCommunications biology2024

An optrode array for spatiotemporally-precise large-scale optogenetic stimulation of deep cortical layers in non-human primates.

Andrew M Clark, Alexander Ingold, Christopher F Reiche, Donald Cundy, Justin L Balsor, Frederick Federer, Niall McAlinden, Yunzhou Cheng, John D Rolston, Loren Rieth and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.2field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Primate neuroethology: a new synthesis.Trends in cognitive sciences · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Journal of neural engineering · 2024
    Article
  17. Applications of 2D Nanomaterials in Neural Interface.International journal of molecular sciences · 2024
    Review
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Andrew M ClarkDepartment of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA.
Alexander IngoldDepartment of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA.
Christopher F ReicheDepartment of Electrical and Computer Engineering, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0001-6216-5888
Donald CundyDepartment of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA.
Justin L BalsorDepartment of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA.
Frederick FedererDepartment of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA.
Niall McAlindenSUPA, Institute of Photonics, Department of Physics, University of Strathclyde, Glasgow, UK.
Yunzhou ChengSUPA, Institute of Photonics, Department of Physics, University of Strathclyde, Glasgow, UK.
John D RolstonDepartments of Neurosurgery and Biomedical Engineering, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0002-8843-5468
Loren RiethMechanical and Aerospace Engineering, West Virginia University, Morgantown, WV, USA.
Martin D DawsonSUPA, Institute of Photonics, Department of Physics, University of Strathclyde, Glasgow, UK.
Keith Mathieson *SUPA, Institute of Photonics, Department of Physics, University of Strathclyde, Glasgow, UK.
Steve Blair *Department of Electrical and Computer Engineering, University of Utah, Salt Lake City, UT, USA. blair@ece.utah.edu.ORCID 0000-0001-5784-590X
Alessandra Angelucci *Department of Ophthalmology and Visual Science, Moran Eye Institute, University of Utah, Salt Lake City, UT, USA. alessandra.angelucci@hsc.utah.edu.ORCID 0000-0002-1957-2231
University of Utah · USUniversity of Strathclyde · GBBrigham and Women's Hospital · USWest Virginia University · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Bryan William Jones · 2005 to 2026
$14.6M
Anatomical and functional organization of inter-areal feedback circuits in the visual cortex, and their impact on neuronal responsesR01EY026812 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI ANGELUCCI, ALESSANDRA · 2016 to 2025
$4.7M
Parallel pathways in visual cortex: functional connectivity of output pathways from area V1 to area V2R01EY019743 · NEI · UNIVERSITY OF UTAH · PI ANGELUCCI, ALESSANDRA · 2009 to 2020
$4.2M
Connectivity and function of inhibitory neurons in the primate visual cortexR01EY031959 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Alessandra Angelucci · 2020 to 2026
$3.0M
Development of an integrated array for simultaneous optogenetic stimulation and electrical recording to study cortical circuit function in the non-human primate brainU01NS099702 · NINDS · UNIVERSITY OF UTAH · PI ANGELUCCI, ALESSANDRA, BLAIR, STEVEN M · 2016 to 2018
$2.4M
NEI NIH HHS P30 EY014800NEI NIH HHS R01 EY019743NEI NIH HHS R01 EY026812NEI NIH HHS R01 EY031959NINDS NIH HHS U01 NS099702
6 · The paper itself

Abstract

Optogenetics has transformed studies of neural circuit function, but remains challenging to apply to non-human primates (NHPs). A major challenge is delivering intense, spatiotemporally-precise, patterned photostimulation across large volumes in deep tissue. Such stimulation is critical, for example, to modulate selectively deep-layer corticocortical feedback circuits. To address this need, we have developed the Utah Optrode Array (UOA), a 10×10 glass needle waveguide array fabricated atop a novel opaque optical interposer, and bonded to an electrically addressable µLED array. In vivo experiments with the UOA demonstrated large-scale, spatiotemporally precise, activation of deep circuits in NHP cortex. Specifically, the UOA permitted both focal (confined to single layers/columns), and widespread (multiple layers/columns) optogenetic activation of deep layer neurons, as assessed with multi-channel laminar electrode arrays, simply by varying the number of activated µLEDs and/or the irradiance. Thus, the UOA represents a powerful optoelectronic device for targeted manipulation of deep-layer circuits in NHP models.

Indexed as

NeuronsOptogeneticsAnimalsElectrodesPrimatesUtah

Identifiers

PMID38485764
PMCPMC10940688
OpenAlexW4392795246

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.